Sponsor:
Ottawa Hospital Research Institute
Code:
NCT03147859
Conditions
HIV-infection/AIDS
Eligibility Criteria
Sex: All
Age: 18 - 65
Healthy Volunteers: Not accepted
Interventions
Vedolizumab (brand name Entyvio)
Brief summary:
Conditions
HIV-infection/AIDS
Study ID
NCT03147859
Start date
Nov 1, 2017
Status verified date
May, 2023
Completion date
Dec 31, 2023
Anticipated
Primary completion date
Dec 31, 2023
Anticipated
Eligibility Criteria
Sex: All
Age: 18 - 65
Healthy Volunteers: Not accepted
Enrollment
10 participants
Anticipated
Allocation
Non randomized
Intervention Model
Sequential
Primary purpose
Treatment
Arms
experimental: Group A-150mg dose of vedolizumab per infusion followed by ATI - Low Dose
experimental: Group B-300mg dose of vedolizumab per infusion followed by ATI - Mid Dose
experimental: Group C-600mg dose of vedolizumab per infusion followed by ATI - High Dose
Interventions
Vedolizumab (brand name Entyvio)
Primary outcome measure
Central contacts
Locations
The Ottawa Hospital -General Campus
Recruiting
Ottawa, Ontario, Canada, K1H 8L6
Contacts
Principal Investigator:
Donald W Cameron, MD
Sponsor
Ottawa Hospital Research Institute
Last update posted
May 11, 2023
Last verified
May, 2023
Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Ottawa Hospital Research Institute on 2023-05-11.